Dufier JL - Search Results

1

[Organic causes of bad visual development in the child].

Roche O, Dufier JL. Roche O, et al. Among authors: dufier jl. Rev Prat. 2007 Nov 30;57(18):2033-8. Rev Prat. 2007. PMID: 18326437 French.

2

[Congenital cataract: general review].

Roche O, Beby F, Orssaud C, Dupont Monod S, Dufier JL. Roche O, et al. Among authors: dufier jl. J Fr Ophtalmol. 2006 Apr;29(4):443-55. doi: 10.1016/s0181-5512(06)77710-5. J Fr Ophtalmol. 2006. PMID: 16885815 Review. French.

3

Familial congenital oculomotor apraxia: clinical and electro-oculographic features.

Orssaud C, Ingster-Moati I, Roche O, Bui Quoc E, Dufier JL. Orssaud C, et al. Among authors: dufier jl. Eur J Paediatr Neurol. 2009 Jul;13(4):370-2. doi: 10.1016/j.ejpn.2008.06.006. Epub 2008 Aug 13. Eur J Paediatr Neurol. 2009. PMID: 18703363

4

Superficial punctate keratitis and conjunctival erosions associated with congenital tufting enteropathy.

Roche O, Putterman M, Salomon J, Lacaille F, Brousse N, Goulet O, Dufier JL. Roche O, et al. Among authors: dufier jl. Am J Ophthalmol. 2010 Jul;150(1):116-121.e1. doi: 10.1016/j.ajo.2010.01.034. Epub 2010 May 5. Am J Ophthalmol. 2010. PMID: 20447614

5

Identification of four new PITX2 gene mutations in patients with Axenfeld-Rieger syndrome.

Vieira V, David G, Roche O, de la Houssaye G, Boutboul S, Arbogast L, Kobetz A, Orssaud C, Camand O, Schorderet DF, Munier F, Rossi A, Delezoide AL, Marsac C, Ricquier D, Dufier JL, Menasche M, Abitbol M. Vieira V, et al. Among authors: dufier jl. Mol Vis. 2006 Dec 1;12:1448-60. Mol Vis. 2006. PMID: 17167399 Free article.

6

Three new PAX6 mutations including one causing an unusual ophthalmic phenotype associated with neurodevelopmental abnormalities.

Dansault A, David G, Schwartz C, Jaliffa C, Vieira V, de la Houssaye G, Bigot K, Catin F, Tattu L, Chopin C, Halimi P, Roche O, Van Regemorter N, Munier F, Schorderet D, Dufier JL, Marsac C, Ricquier D, Menasche M, Penfornis A, Abitbol M. Dansault A, et al. Among authors: dufier jl. Mol Vis. 2007 Apr 2;13:511-23. Mol Vis. 2007. PMID: 17417613 Free PMC article.

7

Novel human pathological mutations. Gene symbol: FZD4. Disease: familial exudative vitreoretinopathy.

Vieira V, de la Houssaye G, Dansault A, Perez E, Roche O, Dufier JL, Marsac C, Menasche M, Abitbol M. Vieira V, et al. Among authors: dufier jl. Hum Genet. 2007 Jun;121(5):650. Hum Genet. 2007. PMID: 17879448 No abstract available.

8

Asymptomatic atrophy of the temporal median raphe of the retina associated with cerebral vasculopathy in homozygous sickle cell disease.

Robert MP, Ingster-Moati I, Roche O, Boddaert N, de Montalembert M, Brousse V, Kossorotoff M, Dufier JL, Faure C. Robert MP, et al. Among authors: dufier jl. J AAPOS. 2012 Aug;16(4):394-7. doi: 10.1016/j.jaapos.2012.03.006. J AAPOS. 2012. PMID: 22929454

9

Ophthalmologic findings in suspected child abuse victims with subdural hematomas.

Pierre-Kahn V, Roche O, Dureau P, Uteza Y, Renier D, Pierre-Kahn A, Dufier JL. Pierre-Kahn V, et al. Among authors: dufier jl. Ophthalmology. 2003 Sep;110(9):1718-23. doi: 10.1016/S0161-6420(03)00581-5. Ophthalmology. 2003. PMID: 13129868

10

[Characteristics of retinal detachment in children].

Bourges JL, Dureau P, Uteza Y, Roche O, Dufier JL. Bourges JL, et al. Among authors: dufier jl. J Fr Ophtalmol. 2001 Apr;24(4):371-7. J Fr Ophtalmol. 2001. PMID: 11351209 French.

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